Product Details

SNP ID

rs200032909

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:65014400 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTTGCTGGTCCCGGCGTTTGTTCC[A/G]GAAACATTCCACCAGGAATTTTTGG

Phenotype

MIM: 604406

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

GNA13 PubMed Links

Gene Details

Gene

GNA13

Gene Name

G protein subunit alpha 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282425.1	890	Missense Mutation	CGG,TGG	R236W	NP_001269354.1
NM_006572.5	890	Missense Mutation	CGG,TGG	R331W	NP_006563.2
XM_011524202.1	890	Intron			XP_011522504.1

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